With Nature stating that almost 60% of clinical professionals expect eConsent adoption to continue post-pandemic, it is clear the benefits behind a digitally-enabled consent process have garnered trust. But a recent Medable poll found that the informed consent process still remains rooted in paper. This reliance on paper comes at a cost though: low enrollment, poor patient retention and issues around site compliance leading to inspection findings and costly trial delays.
In this on-demand webinar, you will learn:
- Common myths that continue to persist around eConsent
- How to improve comprehension with patient-centric consent
- How to use a digital consent management tool to improve trial compliance, quality and oversight